Clark J M, Olsen S J, Weinberg D S, Dalvi M, Whitney R R, Bonner D P, Sykes R B
Antimicrob Agents Chemother. 1987 Feb;31(2):226-9. doi: 10.1128/AAC.31.2.226.
Tigemonam, a new monobactam with excellent activity against gram-negative bacteria, was evaluated for in vivo efficacy and absorption after oral administration to laboratory animals. Tigemonam is absorbed when administered orally to mice and dogs. In a variety of gram-negative systemic infections in mice, orally administered tigemonam was efficacious in all infections studied. Comparison drugs such as amoxicillin, cephalexin, and cefaclor were less efficacious, especially in infections caused by beta-lactamase-producing organisms. In localized infections, tigemonam also demonstrated excellent in vivo activity. In acute pyelonephritis in mice caused by Escherichia coli or Proteus sp., tigemonam was very effective. In a rat lung model with Klebsiella pneumoniae, tigemonam was active with a median effective dose of 46 mg/kg compared with 160 mg/kg for cefaclor and over 200 mg/kg for amoxicillin. Tigemonam was well absorbed in laboratory animals and with its excellent gram-negative spectrum of activity should prove of value in oral antibiotic therapy in humans.
替吉莫南是一种对革兰氏阴性菌具有优异活性的新型单环β-内酰胺类抗生素,我们对其在实验动物口服给药后的体内疗效和吸收情况进行了评估。替吉莫南经口服给予小鼠和犬后可被吸收。在小鼠的多种革兰氏阴性菌全身性感染中,口服替吉莫南对所有研究的感染均有效。诸如阿莫西林、头孢氨苄和头孢克洛等对照药物疗效较差,尤其是在由产β-内酰胺酶的微生物引起的感染中。在局部感染中,替吉莫南也显示出优异的体内活性。在由大肠杆菌或变形杆菌属引起的小鼠急性肾盂肾炎中,替吉莫南非常有效。在肺炎克雷伯菌感染的大鼠肺部模型中,替吉莫南具有活性,其半数有效剂量为46mg/kg,而头孢克洛为160mg/kg,阿莫西林超过200mg/kg。替吉莫南在实验动物中吸收良好,凭借其优异的革兰氏阴性菌活性谱,在人类口服抗生素治疗中应具有价值。